ADHDgene Database
  • Published Variant
  • Published Gene: 359
  • Published Region: 128
  • Pathway by PBA: 8
  • Study: 361

SNP Report

Basic Info
Name rs821577 dbSNP Ensembl
Location chr1:232067057(Fwd)
Variant Alleles T/G
Ancestral Allele G
Functional Annotation intron_variant; nc_transcript_variant; NMD_transcript_variant.
Consequence to Transcript intron_variant(ENST00000366637; ENST00000422590; ENST00000427560; ENST00000439617; ENST00000456782; ENST00000535983; ENST00000537876)
nc_transcript_variant(ENST00000427560; ENST00000456782)
NMD_transcript_variant(ENST00000422590)
No. of Studies 1 (significant: 0; non-significant: 1; trend: 0)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Jacobsen, K. K.,2013 chi-square tests P-value=0.18 (OR=0.89;95%CI=0.76-1.05) chi-square tests P-value=0.18 (OR=0.89;95%CI=0.76-1.05) This SNP was not significant associated with ADHD This SNP was not significant associated with ADHD Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs821577 (count: 4) View in gBrowse (chr1:232056230..232073128 )
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.

Literature-origin SNPs (count: 0)

LD-proxies (count: 4)